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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5564983copy number variation1nstd207human GRCh38 chr7: 57,116,581-57,118,562 , GRCh37.p13 chr7|NW_003571039.1: 348,679-350,660 , GRCh37.p13 chr7: 57,184,288-57,186,269 ZNF479
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5482153copy number variation1nstd206human GRCh38 chr7: 56,993,800-57,540,242 , GRCh37.p13 chr7: 57,190,580-57,599,948 , MTCYBP29, 39 more genes
    nsv5239881copy number variation1nstd204human GRCh38.p13 chr7: 57,124,401-57,127,700 , GRCh37.p13 chr7: 57,192,108-57,195,407 ZNF479
    nsv5228777copy number variation1nstd204human GRCh38.p13 chr7: 57,124,347-57,126,545 , GRCh37.p13 chr7: 57,192,054-57,194,252 ZNF479
    nsv5227661copy number variation1nstd204human GRCh38.p13 chr7: 57,124,709-57,126,779 , GRCh37.p13 chr7: 57,192,416-57,194,486 ZNF479
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956891copy number variation1nstd200human GRCh38 chr7: 57,056,195-63,228,539 , GRCh37.p13 chr7: 57,190,578-62,688,917 , SEPTIN7P15, 50 more genes
    nsv4765725inversion1nstd199human GRCh37 chr7: 57,119,077-62,979,736 , GRCh38.p12 chr7: 57,051,370-63,519,358 , ZNF479, 70 more genes
    nsv4761040inversion1nstd199human GRCh37 chr7: 55,830,732-65,288,125 , GRCh38.p12 chr7: 55,763,039-65,823,138 , CCT6A, 247 more genes
    nsv4684255copy number variation1nstd102humanUncertain significance GRCh37 chr7: 57,127,051-57,528,311 , GRCh38.p12 chr7: 57,059,344-57,468,605 MTATP6P8, NMTRQ-TTG13-1, 33 more genes
    nsv4679115copy number variation1nstd189human GRCh37.p13 chr7: 56,818,765-57,582,095 , GRCh38.p12 chr7: 56,751,072-57,522,389 , ZNF479, 53 more genes
    nsv4612767copy number variation1nstd183human GRCh37 chr7: 56,701,214-58,007,147 , GRCh38.p12 chr7: 56,633,521-57,947,441 , LOC105375289, 66 more genes
    nsv4608784copy number variation1nstd183human GRCh37 chr7: 56,697,186-58,019,983 , GRCh38.p12 chr7: 56,629,493-57,960,277 , VN1R26P, 67 more genes
    nsv4604087copy number variation1nstd183human GRCh37 chr7: 57,130,914-57,863,811 , GRCh38.p12 chr7: 57,063,207-57,804,105 , SAPCD2P2, 40 more genes
    nsv4601829copy number variation1nstd183human GRCh37 chr7: 57,205,767-57,299,345 , GRCh38.p12 chr7: 57,138,060-57,231,638 , MTND4P4, 23 more genes
    nsv4524670copy number variation1nstd166human GRCh37.p13 chr7: 57,148,899-57,248,000 , GRCh38.p12 chr7: 57,081,192-57,180,293 , VN1R27P, 10 more genes
    nsv4523804copy number variation1nstd166human GRCh37.p13 chr7: 57,139,998-57,606,000 , GRCh38.p12 chr7: 57,072,291-57,546,294 , VN1R28P, 36 more genes
    nsv4455806copy number variation1nstd102humanUncertain significance GRCh37 chr7: 52,809,787-58,025,873 , GRCh38.p12 chr7: 52,742,093-57,966,167 RPL31P35, SEC61G, 161 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
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